pantoprazole sodium

Generic: pantoprazole sodium

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler northstar rx llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pantoprazole sodium 40 mg/10mL

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-128
Product ID 72603-128_e6f21248-e12b-4d74-a573-52b189338de2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215860
Listing Expiration 2026-12-31
Marketing Start 2022-08-29

Pharmacologic Class

Classes
proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603128
Hyphenated Format 72603-128

Supplemental Identifiers

RxCUI
283669
UPC
0372603128109
UNII
6871619Q5X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name pantoprazole sodium (source: ndc)
Generic Name pantoprazole sodium (source: ndc)
Application Number ANDA215860 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/10mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (72603-128-10) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-128-01)
source: ndc

Packages (1)

72603-128-10 10 VIAL, SINGLE-DOSE in 1 CARTON (72603-128-10) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-128-01)

Ingredients (1)

pantoprazole sodium (40 mg/10mL)

Linked Drug Pages (1)

Pantoprazole Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e6f21248-e12b-4d74-a573-52b189338de2", "openfda": {"upc": ["0372603128109"], "unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["7e0c5dac-6832-4692-b012-ca59d5e88987"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72603-128-10)  / 10 mL in 1 VIAL, SINGLE-DOSE (72603-128-01)", "package_ndc": "72603-128-10", "marketing_start_date": "20220829"}], "brand_name": "Pantoprazole Sodium", "product_id": "72603-128_e6f21248-e12b-4d74-a573-52b189338de2", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72603-128", "generic_name": "Pantoprazole Sodium", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA215860", "marketing_category": "ANDA", "marketing_start_date": "20220829", "listing_expiration_date": "20261231"}